Versatility of Weinreb amides in the Knorr pyrrole synthesis

DOI: 10.1016/S0040-4020(99)00289-6

Source and publish data:

Tetrahedron p. 6555 - 6566 (1999)

Update date:2022-08-04

Topics:

Authors:

Alberola, Angel

Ortega, Alfonso Gonzalez

Sadaba, M. Luisa

Sanudo, Carmen

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Article abstract of DOI:10.1016/S0040-4020(99)00289-6

N-Methoxy-N-methyl-α-enaminocarboxamides were prepared starting from enamines and Weinreb α-aminoamides. Their reaction with oganometallic compounds and subsequent cyclization constitute a versatile alternative in the Knorr pyrrole synthesis.

Full text of DOI:10.1016/S0040-4020(99)00289-6

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Product name:N,3-dimethyl-N-methoxy-2-(1-methyl-3-oxo-3-phenyl-1-propenylamino)butyramide

Cas No:231609-72-6

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